Please correct answer and don't use hand rating 3. A chemist wants to make the following compound, but is unsure how to do this. Given your excellent education at Valpo,you think carefully about this and decide that you probably can propose a way of making this compound via a substitutionreaction. Propose starting materials and solvent for the necessary reaction.NH

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Answered: 3. A chemist wants to make the…

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.50P

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The dehydration of compound A produces many different products. One of the products formed is compound G. Can you figure out the mechanism? The mechanism proceeds through five intermediates (compounds B-F). Sort the intermediates according to the reaction mechanism which includes a methyl shift, a hydride shift and a resonance structure. Note: treat resonance structures as individual steps. Compound III Compound IV Compound II Compound I Compound V Your answer compound A OH compound G intermediates II
4. As shown below, compound 2 can be made from compound 1 in two steps. Provide the reagents, A, and draw the product B for the first step. Then, provide the reagents C that lead to the final product. (Hint: Product B has a peak in its 'H NMR spectrum at 11.1 ppm that integrates to 1H.) 1 OH A C B
Synthesis: make the following compounds from given materials (on the left) and any other reagents that you need.
9) Suppose I want to perform a simple substitution reaction, replacing the OH with a Cl in the following compound. Which of the following reagents works best? Explain (and that means explain why the wrong answers are wrong as well as why the right answer is right). Option A: Addition of HBr Option B: Addition of SOC12/pyridine Option C: Addition of SOCl2 only OH ? J1
Predict the major products of each reaction.
7. Provide the synthesis for the following product starting with the provide starting material. More than one step is required. Show the mechanism for each reaction. CI- Cl- Starting Material Product
Help with question #14
Propose a mechanism, draw and show all arrows correctly.
Part 3?
In each reaction box, place the best reagent and conditions from the list below. Can't seem to understand this problem. Please help.
1. Prepare the following compounds from any simple alkyl halide having four carbons or less (can be branched, but no other functional groups), ethylene oxide, cyclohexane, and/or cyclopentane. Any other carbon-containing reactants must be synthesized from the above mentioned reagents! Show all steps and reagents. ok
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